المؤلفون: Suissa, M., Place, C., Goillot, E., Freyssingeas, E.

المصدر: The European Physical Journal E: Soft Matter. August 2008 26(4):435-448

المؤلفون: Touraine, J. -L., Laplace, S., Rezzoug, F., Sanhadji, K., Veyron, P., Royo, C., Maire, I., Zabot, M. T., Vanier, M. T., Rolland, M. O., Goillot, E., de Bouteiller, O., Garnier, J. L., Pouteil-Noble, C., Raffaele, P., Livrozet, J. M., Saint-Marc, T.

المصدر: Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. July 1991 14(4):619-626

المؤلفون: Thivolet, C. H., Goillot, E., Bedossa, P., Durand, A., Bonnard, M., Orgiazzi, J.

المصدر: Diabetologia: Clinical and Experimental Diabetes and Metabolism. May 1991 34(5):314-319

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المؤلفون: Laforet, P., Inoue, M., Goillot, E., Lefeuvre, C., Cagin, U., Streichenberger, N., Leonard-Louis, S., Brochier, G., Madelaine, A., Labasse, C., Oldfors Hedberg, Carola, 1969, Krag, T., Jauze, L., Fabregue, J., Labrune, P., Milisenda, J., Nadaj-Pakleza, A., Sacconi, S., Mingozzi, F., Ronzitti, G., Petit, F., Schoser, B., Oldfors, Anders, 1951, Vissing, J., Romero, N. B., Nishino, I., Malfatti, E.

المصدر: Acta Neuropathologica Communications. 7(1)

مصطلحات موضوعية: Cell and Molecular Biology, Cell- och molekylärbiologi, Neurosciences, Neurovetenskaper, Glycogen storage disease III, Muscle glycogenosis, Metabolic myopathies, Myopathology, Autophagy, Autophagic impairment, disease type-iii, phenotype, genotype, Neurosciences & Neurology

URL الوصول: https://gup.ub.gu.se/publication/289406

المؤلفون: Malfatti, E., Goillot, E., Streichenberger, N., Leonard-Louis, S., Brochier, G., Madelaine, A., Labasse, C., Nadaj-Pakleza, A., Sacconi, S., Schoser, B., Oldfors, A., Eymard, B., Romero, N., Vissing, J., Laforêt, P.

المصدر: In Neuromuscular Disorders October 2017 27 Supplement 2:S205-S206

المؤلفون: Chevessier, F., Faraut, B., Ravel-Chapuis, A., Richard, P., Gaudon, K., Bauché, S., Prioleau, C., Herbst, R., Goillot, E., Ioos, C., Azulay, J. P., Attarian, S., Leroy, J. P., Fournier, E., Legay, C., laurent schaeffer, Koenig, J., Fardeau, M., Eymard, B., Pouget, J., Hantaï, D.

المصدر: Scopus-Elsevier

مصطلحات موضوعية: Myasthenic Syndromes, Congenital, DNA Mutational Analysis, Mutation, Missense, Humans, Receptor Protein-Tyrosine Kinases, Receptors, Cholinergic, Frameshift Mutation

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2185cf9f5ec651ab4fe42e20f79bba34
https://pubmed.ncbi.nlm.nih.gov/16550915

المؤلفون: Chevassier, F., Faraut, B., Ravel-Chapuis, A., Richard, Patrick, Gaudron, K., Bauche, S., Prioleau, C., Herbst, R., Goillot, E., Loos, C., Jp, Azulay, Attarian, Shahram, Jp, Leroy, Fournier, E., Legay, C., Schaeffer, L., Eymard, B., Pouget, Jean, Hantai, D.

المساهمون: Plasticité et physio-pathologie de la motricité (P3M) (PPPMP), Université de la Méditerranée - Aix-Marseille 2-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université de la Méditerranée - Aix-Marseille 2, Ruemgardt, Joelle

المصدر: Human Molecular Genetics
Human Molecular Genetics, 2005, pp.964
Human Molecular Genetics, Oxford University Press (OUP), 2005, pp.964

مصطلحات موضوعية: [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], [SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1c7f2f1158b402fe2086576fe018cedb
https://hal.science/hal-00143727

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المؤلفون: Vo-Dinh, Tuan, Lakowicz, Joseph R., Streppa, L., Berguiga, L., Boyer Provera, E., Ratti, F., Goillot, E., Martinez Torres, C., Schaeffer, L., Elezgaray, Juan, Arneodo, A., Argoul, F.

المصدر: Proceedings of SPIE; March 2016, Vol. 9724 Issue: 1 p97240G-97240G-10, 9626771p